Title of article :
Harlequin ichthyosis: A case report from Iran
Author/Authors :
Meymandi, Simin S. Pathology and Stem Cell Research Center - Afzalipour Medical School - Kerman University of Medical Sciences, Kerman , Mehrolhasani, Niloofar Department of Dermatology - Afzalipour Medical School - Kerman University of Medical Sciences, Kerman , Ulmer, Marcie Department of Dermatology and Skin Science - University of British Colombia, Vancouver, Canada , Crawford, Richard I. Department of Dermatology and Skin Science - University of British Colombia, Vancouver, Canada
Pages :
3
From page :
139
To page :
141
Abstract :
Harlequin ichthyosis is a rare and exceedingly severe form of congenital ichthyosis with an incidence of approximately 1 in 300,000 births. These patients are at a high risk for neonatal infection and septicemia. Most affected infants die within the first days or weeks of life. We report a male baby born with harlequin ichthyosis. There is limited information regarding the course and prognosis of neonates affected with harlequin ichthyosis. However, it is now evident that these infants, depending on the severity, may have an extended survival potential with intensive supportive measures as well as the addition of retinoids.
Keywords :
ichthyosis , harlequin ichthyois , retinoid
Journal title :
Astroparticle Physics
Serial Year :
2016
Record number :
2480563
Link To Document :
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